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FCC
Section 12 - FCC Statement
CPI has not approved any changes or modifications to the ATLAS H BOARD device. Any
changes or modifications could void the user’s authority to operate the equipment. See 47
CFR Sec. 15.21
.
USA:
May contain FCC ID: R17LE910SVL
This device complies with 47 CFR Part of the FCC rules. Operation is subject to the following
two conditions:
1) This device may not cause interference.
2) This device must accept any interference received, including interference that may cause
undesired operation.
This radio transmitter has been approved to operate with the antenna provided and with the
maximum permissible gain indicated. Antenna types that have a gain into 50Ω greater than
the maximum gain indicated for any antenna type are strictly prohibited for use with this
device.
Max Antenna Gain (dBi) 50Ω
LTE band 4 = 6.0 dBi
LTE band 13 = 9.0 dBi
To be sure that human exposure to RF energy does not exceed the guidelines in the relevant
standard, always follow these instructions:
A minimum of 20cm (8 inches) should be maintained between the antenna and all persons
and must not be co-located or operated in conjunction with any other antenna or
transmitter. Only the antenna(s) supplied with this device are to be used or the user may
void the authority to use this device.
DO NOT hold the antenna when the device is in use. Holding the antenna will affect call
quality and may cause the radio to operate at a higher power level than needed.
GUIDANCE – PACEMAKERS, POTENTIAL INTERFERENECES
Radiofrequency energy (RF) from cell phones can interact with some electronic devices. This
type of interference is called electromagnetic interference (EMI). For this reason, FDA helped
develop a detailed test method to measure EMI of implanted cardiac pacemakers and
defibrillators from cell phones. This test method is now part of a standard sponsored by the
Association for the Advancement of Medical Instrumentation (AAMI). This standard will
allow manufacturers to ensure that cardiac pacemakers and defibrillators are safe from cell
phone EMI.
The FDA continues to monitor the use of cell phones for possible interactions with other
medical devices. Should harmful interference be found to occur, FDA will conduct testing to
assess the interference and work to resolve the problem.
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Summary of Contents for COTI
Page 1: ...Part No 403018 Issue April 2021 Technical Manual From software version 3 7 1 ...
Page 2: ......
Page 30: ...Section 3 Programming Mode 20 ...
Page 35: ...Section 4 Customising the User Interface Technical Manual 7 8 9 10 11 25 ...
Page 128: ...Section 8 Espresso System 8 2 1 Espresso Water Flow Diagram 118 ...
Page 148: ...Section 11 Electrical Electronic Diagrams Atlas H Board Pin Connections COTI 138 ...
Page 150: ...Section 11 Electrical Electronic Diagrams Atlas H Board Pin Connections LINEA 9 10 1 140 ...
Page 152: ...Section 11 Electrical Electronic Diagrams 11 8 Input Circuit 1 COTI 142 ...
Page 154: ...Section 11 Electrical Electronic Diagrams 11 10 Input Circuit 1 LINEA 144 ...
Page 156: ...Section 11 Electrical Electronic Diagrams 11 12 Output Circuit 1 COTI 146 ...
Page 158: ...Section 11 Electrical Electronic Diagrams 11 14 Output Circuit 1 LINEA 148 ...
Page 168: ...NOTES 158 ...
Page 169: ......